CHEBI:66035 - (1R,4S)-1-hydroperoxy-p-menth-2-en-8-ol acetate

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ChEBI Name (1R,4S)-1-hydroperoxy-p-menth-2-en-8-ol acetate
ChEBI ID CHEBI:66035
ChEBI ASCII Name (1R,4S)-1-hydroperoxy-p-menth-2-en-8-ol acetate
Definition A p-menthane monoterpenoid that is p-menth-2-ene substituted by a hydroperoxy group at position 1 and an acetyloxy group at position 8 (the 1R,4S stereoisomer). Isolated from the leaves of Laurus nobilis, it exhibits trypanocidal activity.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C12H20O4
Net Charge 0
Average Mass 228.28480
Monoisotopic Mass 228.13616
InChI InChI=1S/C12H20O4/c1-9(13)15-11(2,3)10-5-7-12(4,16-14)8-6-10/h5,7,10,14H,6,8H2,1-4H3/t10-,12+/m1/s1
InChIKey VIUQTXYGNHOJBD-PWSUYJOCSA-N
SMILES CC(=O)OC(C)(C)[C@H]1CC[C@@](C)(OO)C=C1
Metabolite of Species Details
Laurus nobilis (NCBI:txid85223) Found in leaf (BTO:0000713). See: PubMed
Roles Classification
Biological Role(s): trypanocidal drug
A drug used to treat or prevent infections caused by protozoal organisms belonging to the suborder Trypanosomatida.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
Application(s): trypanocidal drug
A drug used to treat or prevent infections caused by protozoal organisms belonging to the suborder Trypanosomatida.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (1R,4S)-1-hydroperoxy-p-menth-2-en-8-ol acetate (CHEBI:66035) has role metabolite (CHEBI:25212)
(1R,4S)-1-hydroperoxy-p-menth-2-en-8-ol acetate (CHEBI:66035) has role trypanocidal drug (CHEBI:36335)
(1R,4S)-1-hydroperoxy-p-menth-2-en-8-ol acetate (CHEBI:66035) is a p-menthane monoterpenoid (CHEBI:25186)
(1R,4S)-1-hydroperoxy-p-menth-2-en-8-ol acetate (CHEBI:66035) is a acetate ester (CHEBI:47622)
(1R,4S)-1-hydroperoxy-p-menth-2-en-8-ol acetate (CHEBI:66035) is a peroxol (CHEBI:35924)
IUPAC Name
2-[(1S,4R)-4-hydroperoxy-4-methylcyclohex-2-en-1-yl]propan-2-yl acetate
Registry Number Type Source
9260434 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
12419922 PubMed citation Europe PMC
Last Modified
25 February 2013